ChemicalBook CAS DataBase List Benzaldehyde

Benzaldehyde synthesis

13synthesis methods

Product Name:Benzaldehyde
CAS Number:100-52-7
Molecular formula:C7H6O
Molecular Weight:106.12

Benzaldehyde is prepared by hydrolysis of benzal chloride, for example, in acidic media in the presence of a catalyst such as ferric chloride or in alkaline media with aqueous sodium carbonate. Part of the commercially available benzaldehyde originates from a technical process for phenol. In this process, benzaldehyde is a by-product in the oxidation, in air, of toluene to benzoic acid.

98-95-3
7 suppliers
$14.00/25g

100-51-6 Synthesis

100-51-6
1356 suppliers
$5.00/100g

538-51-2 Synthesis

538-51-2
97 suppliers
$45.00/1g

100-52-7
952 suppliers
$20.37/250g

Yield:538-51-2 100%

Reaction Conditions:

with (trifluoromethyl)benzene;titanium(IV) dioxide in dodecane; under 750.075 Torr; for 3 h;Darkness;Inert atmosphere;Irradiation;Reagent/catalyst;

Steps:

2.2. Typical experimental procedure for photocatalytic test

General procedure: In a typical procedure, 40 mg of TiO2, 31 mL (0.3 mmol) of benzylalcohol and 10 mL (0.1 mmol) of nitrobenzene were added into10 mL of reagent grade benzotrifluoride (BTF), n-dodecane wasused as an internal standard. The mixture was evacuated and backfilledwith N2 (1.0 atm) five times to completely remove air andallowed to stir for 30 min in the dark. The reaction mixture wasthen magnetically stirred at 800 rpm and illuminated by the 300-WXenon Illuminator System with an CM 1 filter in the wavelengthregion of 380-760 nm. At a certain time after the photocatalyticreaction, an aliquot of the reaction solutions (60 mL) were pulledout, filtered by a one-time plastic filter and diluted by 0.5 mL ethanolfor gas chromatograph analysis (Agilent 7890A equipped withan FID detector). The conversion of alcohol, nitrobenzene, and yieldof aldehyde and aniline were defined as follows:

References:

Yang, Xue;Tao, Huilin;Leow, Wan Ru;Li, Jingjun;Tan, Yanxi;Zhang, Yongfan;Zhang, Teng;Chen, Xiaodong;Gao, Shuiying;Cao, Rong [Journal of Catalysis,2019,vol. 373,p. 116 - 125]